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FDA 510(k)

SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR

K-Number: K813447 · 1981-12-31

Decision Date1981-12-31
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR is the device name listed in this FDA 510(k) record. The listed applicant is Rna Medical Corp.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813447. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR?

SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Rna Medical Corp.. The 510(k) number is K813447.

When did SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR receive FDA 510(k) clearance?

SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813447.

Who is the listed applicant for SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR?

The FDA 510(k) record lists Rna Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR?

The FDA product code for SOLUTIONS & BUFFERS FOR BLOOD GAS INSTR is JIS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Rna Medical Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JIS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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